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137 nile red  (Beyotime)


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    Structured Review

    Beyotime 137 nile red
    137 Nile Red, supplied by Beyotime, used in various techniques. Bioz Stars score: 99/100, based on 35 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/red+fluorescence/Lipid+Droplets+Red+Fluorescence+Assay+Kit+with+Nile+Red/pm42887812-76-5-8
    Average 99 stars, based on 35 article reviews
    137 nile red - by Bioz Stars, 2026-10
    99/100 stars

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    Related Articles

    Cell Culture:

    Article Title: ZBED6 deficiency drives pathological cardiac hypertrophy through MEOX1-ERK1/2-dependent autophagy dysfunction.
    Article Snippet: .. Apoptosis in cultured cardiomyocytes and cardiac tissues was detected using a One Step TUNEL Apoptosis Assay Kit with red fluorescence (Beyotime Biotechnology, C1089) according to the manufacturer’s instructions. ..

    TUNEL Assay:

    Article Title: ZBED6 deficiency drives pathological cardiac hypertrophy through MEOX1-ERK1/2-dependent autophagy dysfunction.
    Article Snippet: .. Apoptosis in cultured cardiomyocytes and cardiac tissues was detected using a One Step TUNEL Apoptosis Assay Kit with red fluorescence (Beyotime Biotechnology, C1089) according to the manufacturer’s instructions. ..

    Apoptosis Assay:

    Article Title: ZBED6 deficiency drives pathological cardiac hypertrophy through MEOX1-ERK1/2-dependent autophagy dysfunction.
    Article Snippet: .. Apoptosis in cultured cardiomyocytes and cardiac tissues was detected using a One Step TUNEL Apoptosis Assay Kit with red fluorescence (Beyotime Biotechnology, C1089) according to the manufacturer’s instructions. ..

    Fluorescence:

    Article Title: ZBED6 deficiency drives pathological cardiac hypertrophy through MEOX1-ERK1/2-dependent autophagy dysfunction.
    Article Snippet: .. Apoptosis in cultured cardiomyocytes and cardiac tissues was detected using a One Step TUNEL Apoptosis Assay Kit with red fluorescence (Beyotime Biotechnology, C1089) according to the manufacturer’s instructions. ..

    Article Title: Dietary Cottonseed Protein Substituting Fish Meal Induces Hepatic Ferroptosis Through SIRT1-YAP-TRFC Axis in Micropterus salmoides : Implications for Inflammatory Regulation and Liver Health
    Article Snippet: Fresh liver tissues (100 mg each) were obtained from fish in all CP groups following deep anesthesia and then cut into pieces using scissors before mitochondrial isolation using a commercial kit (Beyotime, Catalog No. C3606, Beyotime Biotechnology, Shanghai, China). .. The MMP assay was conducted using the JC-1 fluorescent probe method (Beyotime, Catalog No. C2006) for rapid visualization in the dark using green and red fluorescence (Ex = 490 nm and Em = 530 nm for JC-1 monomers; Ex = 525 nm and Em = 590 nm for J-aggregates). ..

    Article Title: Astrocytic GSTM2-STAT3 Interaction Ameliorates the Diabetes Associated Cognitive Dysfunction via Targeting Mitochondrial Defects and Oxidative Stress
    Article Snippet: .. The assessment of mitochondrial membrane potential was carried out by calculating the ROS detector (JC-1, C2006, Beyotime Biotech Inc) by comparing the levels of green fluorescence (JC-1 monomer) at 530 nm with those of red fluorescence (JC-1 polymer) at 590 nm. ..

    Article Title: Astrocytic GSTM2-STAT3 interaction ameliorates the diabetes associated cognitive dysfunction via targeting mitochondrial defects and oxidative stress
    Article Snippet: .. The assessment of mitochondrial membrane potential was carried out by calculating the ROS detector (JC-1, C2006, Beyotime Biotech Inc) by comparing the levels of green fluorescence (JC-1 monomer) at 530 nm with those of red fluorescence (JC-1 polymer) at 590 nm. ..

    Article Title: Dietary Cottonseed Protein Substituting Fish Meal Induces Hepatic Ferroptosis Through SIRT1-YAP-TRFC Axis in Micropterus salmoides : Implications for Inflammatory Regulation and Liver Health.
    Article Snippet: Fresh liver tissues (100 mg each) were obtained from fish in all CP groups following deep anesthesia and then cut into pieces using scissors before mitochondrial isolation using a commercial kit (Beyotime, Catalog No. C3606, Beyotime Biotechnology, Shanghai, China). .. The MMP assay was conducted using the JC-1 fluorescent probe method (Beyotime, Catalog No. C2006) for rapid visualization in the dark using green and red fluorescence (Ex = 490 nm and Em = 530 nm for JC-1 monomers; Ex = 525 nm and Em = 590 nm for J-aggregates). ..

    Mmp Assay:

    Article Title: Dietary Cottonseed Protein Substituting Fish Meal Induces Hepatic Ferroptosis Through SIRT1-YAP-TRFC Axis in Micropterus salmoides : Implications for Inflammatory Regulation and Liver Health
    Article Snippet: Fresh liver tissues (100 mg each) were obtained from fish in all CP groups following deep anesthesia and then cut into pieces using scissors before mitochondrial isolation using a commercial kit (Beyotime, Catalog No. C3606, Beyotime Biotechnology, Shanghai, China). .. The MMP assay was conducted using the JC-1 fluorescent probe method (Beyotime, Catalog No. C2006) for rapid visualization in the dark using green and red fluorescence (Ex = 490 nm and Em = 530 nm for JC-1 monomers; Ex = 525 nm and Em = 590 nm for J-aggregates). ..

    Article Title: Dietary Cottonseed Protein Substituting Fish Meal Induces Hepatic Ferroptosis Through SIRT1-YAP-TRFC Axis in Micropterus salmoides : Implications for Inflammatory Regulation and Liver Health.
    Article Snippet: Fresh liver tissues (100 mg each) were obtained from fish in all CP groups following deep anesthesia and then cut into pieces using scissors before mitochondrial isolation using a commercial kit (Beyotime, Catalog No. C3606, Beyotime Biotechnology, Shanghai, China). .. The MMP assay was conducted using the JC-1 fluorescent probe method (Beyotime, Catalog No. C2006) for rapid visualization in the dark using green and red fluorescence (Ex = 490 nm and Em = 530 nm for JC-1 monomers; Ex = 525 nm and Em = 590 nm for J-aggregates). ..

    Membrane:

    Article Title: Astrocytic GSTM2-STAT3 Interaction Ameliorates the Diabetes Associated Cognitive Dysfunction via Targeting Mitochondrial Defects and Oxidative Stress
    Article Snippet: .. The assessment of mitochondrial membrane potential was carried out by calculating the ROS detector (JC-1, C2006, Beyotime Biotech Inc) by comparing the levels of green fluorescence (JC-1 monomer) at 530 nm with those of red fluorescence (JC-1 polymer) at 590 nm. ..

    Article Title: Astrocytic GSTM2-STAT3 interaction ameliorates the diabetes associated cognitive dysfunction via targeting mitochondrial defects and oxidative stress
    Article Snippet: .. The assessment of mitochondrial membrane potential was carried out by calculating the ROS detector (JC-1, C2006, Beyotime Biotech Inc) by comparing the levels of green fluorescence (JC-1 monomer) at 530 nm with those of red fluorescence (JC-1 polymer) at 590 nm. ..

    Polymer:

    Article Title: Astrocytic GSTM2-STAT3 Interaction Ameliorates the Diabetes Associated Cognitive Dysfunction via Targeting Mitochondrial Defects and Oxidative Stress
    Article Snippet: .. The assessment of mitochondrial membrane potential was carried out by calculating the ROS detector (JC-1, C2006, Beyotime Biotech Inc) by comparing the levels of green fluorescence (JC-1 monomer) at 530 nm with those of red fluorescence (JC-1 polymer) at 590 nm. ..

    Article Title: Astrocytic GSTM2-STAT3 interaction ameliorates the diabetes associated cognitive dysfunction via targeting mitochondrial defects and oxidative stress
    Article Snippet: .. The assessment of mitochondrial membrane potential was carried out by calculating the ROS detector (JC-1, C2006, Beyotime Biotech Inc) by comparing the levels of green fluorescence (JC-1 monomer) at 530 nm with those of red fluorescence (JC-1 polymer) at 590 nm. ..



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    Image Search Results


    YME1L1 promotes neuronal mitochondrial damage after AD. (A) CCK8 assay for cell viability. (B) Flow cytometry for apoptosis detection. (C) TEM for mitochondrial assessment (The green arrow indicates normal mitochondria, and the red arrow indicates damaged mitochondria). (D) ATP level measurement. (E) JC‐1 staining for cellular mitochondrial membrane potential measurement. (F) MitoSOX fluorescence staining for cellular mitochondrial ROS analysis. n = 3. * p < 0.05; ** p < 0.01; *** p < 0.001; **** p < 0.0001.

    Journal: Aging Cell

    Article Title: HNRNPC Succinylation Influences the Neurodegeneration of Alzheimer's Disease Through YME1L1 ‐Mediated Mitochondrial Metabolism

    doi: 10.1111/acel.70646

    Figure Lengend Snippet: YME1L1 promotes neuronal mitochondrial damage after AD. (A) CCK8 assay for cell viability. (B) Flow cytometry for apoptosis detection. (C) TEM for mitochondrial assessment (The green arrow indicates normal mitochondria, and the red arrow indicates damaged mitochondria). (D) ATP level measurement. (E) JC‐1 staining for cellular mitochondrial membrane potential measurement. (F) MitoSOX fluorescence staining for cellular mitochondrial ROS analysis. n = 3. * p < 0.05; ** p < 0.01; *** p < 0.001; **** p < 0.0001.

    Article Snippet: Intracellular superoxide levels were measured using the MitoSOX Red fluorescent probe (HY‐D1055; MCE, USA).

    Techniques: CCK-8 Assay, Flow Cytometry, Staining, Membrane, Fluorescence

    YME1L1 induces neuronal mitochondrial damage and neuronal death following AD through OPA1 hydrolysis. (A) WB detection of OPA1 expression in hippocampal tissue ( n = 6). (B) WB detection of OPA1 expression. (C) CCK8 assay for cell viability. (D) Flow cytometry for apoptosis detection. (E) TEM for mitochondrial detection (The red arrow indicates damaged mitochondria). (F) ATP level detection. (G) JC‐1 staining for measuring mitochondrial membrane potential. (H) MitoSOX fluorescence staining for analyzing mitochondrial ROS. n = 3. * p < 0.05; ** p < 0.01; *** p < 0.001; **** p < 0.0001.

    Journal: Aging Cell

    Article Title: HNRNPC Succinylation Influences the Neurodegeneration of Alzheimer's Disease Through YME1L1 ‐Mediated Mitochondrial Metabolism

    doi: 10.1111/acel.70646

    Figure Lengend Snippet: YME1L1 induces neuronal mitochondrial damage and neuronal death following AD through OPA1 hydrolysis. (A) WB detection of OPA1 expression in hippocampal tissue ( n = 6). (B) WB detection of OPA1 expression. (C) CCK8 assay for cell viability. (D) Flow cytometry for apoptosis detection. (E) TEM for mitochondrial detection (The red arrow indicates damaged mitochondria). (F) ATP level detection. (G) JC‐1 staining for measuring mitochondrial membrane potential. (H) MitoSOX fluorescence staining for analyzing mitochondrial ROS. n = 3. * p < 0.05; ** p < 0.01; *** p < 0.001; **** p < 0.0001.

    Article Snippet: Intracellular superoxide levels were measured using the MitoSOX Red fluorescent probe (HY‐D1055; MCE, USA).

    Techniques: Expressing, CCK-8 Assay, Flow Cytometry, Staining, Membrane, Fluorescence

    HNRNPC succinylation modifies neuronal mitochondrial damage and neuronal death following AD via YME1L1. (A) PCR and WB detection of YME1L1, WB detection of OPA1. (B) CCK8 analysis of cell activity. (C) Flow cytometry to detect cell apoptosis. (D) TEM detection of mitochondria (The green arrow points to normal mitochondria, and the red arrow points to damaged mitochondria). (E) ATP level detection. (F) JC‐1 staining was used to measure the mitochondrial membrane potential of cells. (G) MitoSOX fluorescent staining analysis of mitochondrial ROS in cells. n = 3. * p < 0.05; ** p < 0.01; *** p < 0.001; **** p < 0.0001.

    Journal: Aging Cell

    Article Title: HNRNPC Succinylation Influences the Neurodegeneration of Alzheimer's Disease Through YME1L1 ‐Mediated Mitochondrial Metabolism

    doi: 10.1111/acel.70646

    Figure Lengend Snippet: HNRNPC succinylation modifies neuronal mitochondrial damage and neuronal death following AD via YME1L1. (A) PCR and WB detection of YME1L1, WB detection of OPA1. (B) CCK8 analysis of cell activity. (C) Flow cytometry to detect cell apoptosis. (D) TEM detection of mitochondria (The green arrow points to normal mitochondria, and the red arrow points to damaged mitochondria). (E) ATP level detection. (F) JC‐1 staining was used to measure the mitochondrial membrane potential of cells. (G) MitoSOX fluorescent staining analysis of mitochondrial ROS in cells. n = 3. * p < 0.05; ** p < 0.01; *** p < 0.001; **** p < 0.0001.

    Article Snippet: Intracellular superoxide levels were measured using the MitoSOX Red fluorescent probe (HY‐D1055; MCE, USA).

    Techniques: Activity Assay, Flow Cytometry, Staining, Membrane

    SIRT5 affects neuronal mitochondrial function by desuccinylating HNRNPC. (A) WB detection of YME1L1 and OPA1 expression. (B) CCK8 analysis of cell activity. (C) Flow cytometry detection of cell apoptosis. (D) TEM detection of mitochondrial morphology (The green arrow points to normal mitochondria, and the red arrow points to damaged mitochondria). (E) ATP level detection. (F) JC‐1 staining to measure cell mitochondrial membrane potential. (G) MitoSOX fluorescent staining analysis of mitochondrial ROS in cells. n = 3. * p < 0.05; ** p < 0.01; *** p < 0.001; **** p < 0.0001; ns stands for no significant difference.

    Journal: Aging Cell

    Article Title: HNRNPC Succinylation Influences the Neurodegeneration of Alzheimer's Disease Through YME1L1 ‐Mediated Mitochondrial Metabolism

    doi: 10.1111/acel.70646

    Figure Lengend Snippet: SIRT5 affects neuronal mitochondrial function by desuccinylating HNRNPC. (A) WB detection of YME1L1 and OPA1 expression. (B) CCK8 analysis of cell activity. (C) Flow cytometry detection of cell apoptosis. (D) TEM detection of mitochondrial morphology (The green arrow points to normal mitochondria, and the red arrow points to damaged mitochondria). (E) ATP level detection. (F) JC‐1 staining to measure cell mitochondrial membrane potential. (G) MitoSOX fluorescent staining analysis of mitochondrial ROS in cells. n = 3. * p < 0.05; ** p < 0.01; *** p < 0.001; **** p < 0.0001; ns stands for no significant difference.

    Article Snippet: Intracellular superoxide levels were measured using the MitoSOX Red fluorescent probe (HY‐D1055; MCE, USA).

    Techniques: Expressing, Activity Assay, Flow Cytometry, Staining, Membrane